Extreme environment surfactant compositions comprising hydrolysis resistant organomodified disiloxane surfactants

ABSTRACT

Compositions comprising an asymmetric disiloxane surfactant composition comprising a silicone composition comprising a silicone having the formula: 
 
MM′
where M or M′ comprises an alkylpolyalkyleneoxide bearing substituent selected from the group consisting of: 
         R 13 (C 2 H 4 O) a (C 3 H 6 O) b (C 4 H 8 O) c R 14  and    R 12 SiR 5 R 6 (R 13 (C 2 H 4 O) a (C 3 H 6 O) b (C 4 H 8 O) c R 14 ) that exhibit resistance to hydrolysis over a wide pH range.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Continuation-In Part application of U.S. Ser. No.11/301,707 filed Dec. 13, 2005 and claims the benefit of U.S.Provisional Application Ser. No. 60/726,409, filed Oct. 13, 2005

FIELD OF THE INVENTION

The present invention relates to extreme environment compositionscomprising disiloxane surfactant compositions that exhibit resistance tohydrolysis over a wide pH range. More particularly the present inventionrelates to such extreme environment compositions having a resistance tohydrolysis between a pH of about 3 to a pH of about 12.

BACKGROUND OF THE INVENTION

The topical application of liquid compositions to the surfaces of bothanimate and inanimate objects to effect a desired change involve theprocesses of controlling wetting, spreading, foaming, detergency, andthe like. When used in aqueous solutions to improve the delivery ofactive ingredients to the surface being treated, trisiloxane typecompounds have been found to be useful in enabling the control of theseprocesses to achieve the desired effect. However, the trisiloxanecompounds may only be used in a narrow pH range, ranging from a slightlyacidic pH of 6 to a very mildly basic pH of 7.5. Outside this narrow pHrange, the trisiloxane compounds are not stable to hydrolysis undergoinga rapid decomposition.

SUMMARY OF THE INVENTION

The present invention provides for an extreme environment compositionuseful as an agricultural composition, a personal care composition, acoating composition or a home care composition, said compositioncomprising a silicone composition comprising a silicone having theformula:MM′where

M=R¹R²R³SiO_(1/2);

M′═R⁴R⁵R⁶SiO_(1/2);

with R¹ selected from the group consisting of branched monovalenthydrocarbon radical of from 3 to 6 carbon atoms and R⁷, where R⁷ isselected from the group consisting of

R⁸R⁹R¹⁰SiR¹² and (R⁴R⁵R⁶)SiR¹²

with R⁸, R⁹, and R¹⁰ each independently selected from the group ofmonovalent hydrocarbon radicals having from 1 to 6 carbon atoms andmonovalent aryl or alkaryl hydrocarbon radicals having from 6 to 13carbon atoms and R¹² is a divalent hydrocarbon radical having from 1 to3 carbon atoms,

R² and R³ are each independently selected from the group of from 1 to 6carbon atom monovalent hydrocarbon radicals or R¹, with R⁴ analkylpolyalkyleneoxide bearing substituent selected from the groupconsisting of:

R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴ and

R¹²SiR⁵R⁶(R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴)

where R¹³ is a divalent linear or branched hydrocarbon radical havingthe structure:

—CH₂—CH(R¹⁵)(R¹⁶)_(d)O—

where R¹⁵ is H or methyl; R¹⁶ is a divalent alkyl radical of 1 to 6carbons where the subscript d may be 0 or 1;

-   R¹⁴ is selected from the group consisting of H, monovalent    hydrocarbon radicals of from 1 to 6 carbon atoms and acetyl where    the subscripts a, b and c are zero or positive and satisfy the    following relationships:    2≦a+b+c≦20 with a ≧2,    and R⁵ and R⁶ are each independently selected from the group of    monovalent hydrocarbon radicals having from 1 to 6 carbon atoms or    R⁴.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, integer values of stoichiometric subscripts refer tomolecular species and non-integer values of stoichiometric subscriptsrefer to a mixture of molecular species on a molecular weight averagebasis, a number average basis or a mole fraction basis.

The present invention provides for a disiloxane compound or compositionsthereof useful as a surfactant having the general formula:MM′where

M=R¹R²R³SiO_(1/2);

M′═R⁴R⁵R⁶SiO_(1/2);

with R¹ a branched monovalent hydrocarbon radical of from 3 to 6 carbonatoms or R⁷, where R⁷ is selected from the group consisting of

R⁸R⁹R¹⁰SiR¹² and (R⁴R⁵R⁶)SiR¹²

with R⁸, R⁹, and R¹⁰ each independently selected from the group ofmonovalent hydrocarbon radicals having from 1 to 6 carbon atoms andmonovalent aryl or alkaryl hydrocarbon radicals having from 6 to 13carbon atoms and R¹² is a divalent hydrocarbon radical having from 1 to3 carbon atoms,

-   -   R² and R³ are each independently selected from the group of from        1 to 6 carbon atom monovalent hydrocarbon radicals or R¹, with        R⁴ an alkylpolyalkyleneoxide bearing substituent selected from        the group consisting of:

R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴ and

R¹²SiR⁵R⁶(R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴)

where R¹³ is a divalent linear or branched hydrocarbon radical havingthe structure:

—CH₂—CH(R¹⁵)(R¹⁶)_(d)O—

where R¹⁵ is H or methyl; R¹⁶ is a divalent alkyl radical of 1 to 6carbons where the subscript d may be 0 or 1;

-   R¹⁴ is selected from the group consisting of H, monovalent    hydrocarbon radicals of from 1 to 6 carbon atoms and acetyl subject    to the limitation that the subscripts a, b and c are zero or    positive and satisfy the following relationships:    2≦a+b+c≦20 with a ≧2,    and R⁵ and R⁶ are each independently selected from the group of    monovalent hydrocarbon radicals having from 1 to 6 carbon atoms or    R⁴. When the subscript a satisfies the condition 2≦a ≦4 it is    advisable to utilize a cosurfactant as hereinafter set forth in    order to obtain the benefit of the compositions of the present    invention.

One method of producing the composition of the present invention is toreact a molecule of the following formula:MM^(H)where M^(H) is the hydride precursor to the M′ structural unit in thecomposition of the present invention, wherein the definitions andrelationships are later defined and consistent with those defined above,under hydrosilylation conditions, with an olefinically modifiedpolyalkyleneoxide, such as allyloxypolyethyleneglycol, ormethallyloxypolyalkyleneoxide, which are incorporated herein asexamples, and not set forth to limit other possible olefinicallymodified alkyleneoxide components. As used herein the phrase“olefinically modified polyalkyleneoxide” is defined as a moleculepossessing one or more alkyleneoxide groups containing one or more,terminal or pendant, carbon-carbon double bonds. The polyether is anolefinically modified polyalkyleneoxide (hereinafter referred to as“polyether”) is described by the general formula:CH₂═CH(R¹⁵)(R¹⁶)_(d)O(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴where

R¹⁵ is H or methyl; R¹⁶ is a divalent alkyl radical of 1 to 6 carbonswhere the subscript d may be 0 or 1; R¹⁴ is H, a monofunctionalhydrocarbon radical of 1 to 6 carbons, or acetyl. When the polyether iscomposed of mixed oxyalkyleneoxide groups (i.e. oxyethylene,oxypropylene and oxybutylene) the units may be blocked, or randomlydistributed. One skilled in the art will understand the advantages ofusing a blocked or random configuration. Illustrative examples ofblocked configurations are: -(oxyethylene)_(a)(oxypropylene)_(b)-;-(oxybutylene)_(c)(oxyethylene)_(a)-; and-(oxypropylene)_(b)(oxyethylene)_(a)(oxybutylene)_(c)-

Illustrative examples of the polyether are provided below, but notlimited to:

CH₂═CHCH₂O(CH₂CH₂O)₈H; CH₂═CHCH₂O(CH₂CH₂O)₈CH₃;

CH₂═CHCH₂O(CH₂CH₂O)₄(CH₂CH(CH₃)O)₅H;

CH₂═CHO(CH₂CH₂O)₅(CH₂CH(CH₃)O)₅H;

CH₂═C(CH₃)CH₂O(CH₂CH₂O)₄(CH₂CH(CH₃)O)₅C(═O)CH₃;

CH₂═CHCH₂O(CH₂CH₂O)₅(CH₂CH(CH₃)O)₂(CH₂CH(CH₂CH₃)O)₂H

Polyether modified siloxanes are prepared in the normal manner throughthe use of a hydrosilylation reaction to graft the olefinically modified(i.e. vinyl, allyl or methallyl) polyalkyleneoxide onto the hydride(SiH) intermediate of the disiloxane of the present invention.

Precious metal catalysts suitable for making polyether-substitutedsiloxanes are also well known in the art and comprise complexes ofrhodium, ruthenium, palladium, osmium, iridium, or platinum. Many typesof platinum catalysts for this SiH olefin addition reaction are knownand such platinum catalysts may be used to generate the compositions ofthe present invention. The platinum compound can be selected from thosehaving the formula (PtCl₂Olefin) and H(PtCl₃Olefin) as described in U.S.Pat. No. 3,159,601, hereby incorporated by reference. A further platinumcontaining material can be a complex of chloroplatinic acid with up to 2moles per gram of platinum of a member selected from the classconsisting of alcohols, ethers, aldehydes and mixtures thereof asdescribed in U.S. Pat. No. 3,220,972 hereby incorporated by reference.Yet another group of platinum containing materials useful in thispresent invention is described in U.S. Pat. Nos. 3,715,334; 3,775,452and 3,814,730 (Karstedt). Additional background concerning the art maybe found in J. L. Spier, “Homogeneous Catalysis of Hydrosilation byTransition Metals”, in Advances in Organometallic Chemistry, volume 17,pages 407 through 447, F.G.A. Stone and R. West editors, published byAcademic Press (New York, 1979). Those skilled in the art can easilydetermine an effective amount of platinum catalyst. Generally aneffective amount ranges from about 0.1 to 50 parts per million of thetotal organomodified disiloxane composition.

The compositions as well as the siloxanes of the present inventionexhibit an enhanced resistance to hydrolysis outside a pH range rangingfrom 6 to 7.5, i.e. in extreme environmental conditions. An extremeenvironment is defined as an aqueous solution pH below 6 or above 7.5 ornon-aqueous equivalents in terms of Bronsted acidity or basicity orLewis acidity ort basicity. Enhanced resistance to hydrolysis can bedemonstrated by a variety of tests but as used herein enhancedresistance to hydrolysis means 50 mole percent or more of the hydrolysisresistant composition of the present invention remains unchanged orunreacted after a period of a twenty-four exposure to aqueous acidicconditions where the solution has a pH lower than 6 or after a period ofa twenty-four hour exposure to aqueous basic conditions where thesolution has a pH greater than 7.5. Under acidic conditions thecompositions of the present invention show a survival of 50 mole percentof the original concentration or greater at a pH of 5 or less for aperiod of time in excess of 48 hours; specifically the compositions ofthe present invention show a survival of 50 mole percent or greater at apH of 5 or less for a period of time in excess of 2 weeks; morespecifically the compositions of the present invention show a survivalof 50 mole percent or greater at a pH of 5 or less for a period of timein excess of 1 month; and most specifically the compositions of thepresent invention show a survival of 50 mole percent or greater at a pHof 5 or less for a period of time in excess of 6 months. Under basicconditions the compositions of the present invention show a survival of50 mole percent or greater at a pH of 8 or more for a period of time inexcess of 2 weeks; specifically the compositions of the presentinvention show a survival of 50 mole percent or greater at a pH of 8 ormore for a period of time in excess of 4 weeks; more specifically thecompositions of the present invention show a survival of 50 mole percentor greater at a pH of 8 or more for a period of time in excess of 6months; and most specifically the compositions of the present inventionshow a survival of 50 mole percent or greater at a pH of 8 or more for aperiod of time in excess of 1 year.

Uses for the Compositions of the Present Invention:

The compositions of the present invention may be utilized in a varietyof forms: as liquid solutions, dispersions of solids in liquids,dispersions of liquids in liquids as the previously described emulsions,solid mixtures or solid solutions either separately or in the formspreviously listed in combination one with the other.

A. Pesticide—Agriculture, Horticulture, Turf, Ornamental and Forestry:

Many pesticide applications require the addition of an adjuvant to thespray mixture to provide wetting and spreading on foliar surfaces. Oftenthat adjuvant is a surfactant, which can perform a variety of functions,such as increasing spray droplet retention on difficult to wet leafsurfaces, enhance spreading to improve spray coverage, or to providepenetration of the herbicide into the plant cuticle. These adjuvants areprovided either as a tank-side additive or used as a component inpesticide formulations.

Typical uses for pesticides include agricultural, horticultural, turf,ornamental, home and garden, veterinary and forestry applications. Thepesticidal compositions of the present invention also include at leastone pesticide, where the organomodified disiloxane surfactant of thepresent invention is present at an amount sufficient to deliver between0.005% and 2% to the final use concentration, either as a concentrate ordiluted in a tank mix. Optionally the pesticidal composition may includeexcipients, cosurfactants, solvents, foam control agents, depositionaids, drift retardants, biologicals, micronutrients, fertilizers and thelike. The term pesticide means any compound used to destroy pests, e.g.,rodenticides, insecticides, miticides, fungicides, and herbicides.Illustrative examples of pesticides that can be employed include, butare not limited to, growth regulators, photosynthesis inhibitors,pigment inhibitors, mitotic disrupters, lipid biosynthesis inhibitors,cell wall inhibitors, and cell membrane disrupters. The amount ofpesticide employed in compositions of the invention varies with the typeof pesticide employed. More specific examples of pesticide compoundsthat can be used with the compositions of the invention are, but notlimited to, herbicides and growth regulators, such as: phenoxy aceticacids, phenoxy propionic acids, phenoxy butyric acids, benzoic acids,triazines and s-triazines, substituted ureas, uracils, bentazon,desmedipham, methazole, phenmedipham, pyridate, amitrole, clomazone,fluridone, norflurazone, dinitroanilines, isopropalin, oryzalin,pendimethalin, prodiamine, trifluralin, glyphosate, sulfonylureas,imidazolinones, clethodim, diclofop-methyl, fenoxaprop-ethyl,fluazifop-p-butyl, haloxyfop-methyl, quizalofop, sethoxydim,dichlobenil, isoxaben, and bipyridylium compounds.

Fungicide compositions that can be used with the present inventioninclude, but are not limited to, aldimorph, tridemorph, dodemorph,dimethomorph; flusilazol, azaconazole, cyproconazole, epoxiconazole,furconazole, propiconazole, tebuconazole and the like; imazalil,thiophanate, benomyl carbendazim, chlorothialonil, dicloran,trifloxystrobin, fluoxystrobin, dimoxystrobin, azoxystrobin, furcaranil,prochloraz, flusulfamide, famoxadone, captan, maneb, mancozeb, dodicin,dodine, and metalaxyl.

Insecticides, including larvacide, miticide and ovacide compounds thatcan be used with the composition of the present invention, but notlimited to, Bacillus thuringiensis, spinosad, abamectin, doramectin,lepimectin, pyrethrins, carbaryl, primicarb, aldicarb, methomyl,amitraz, boric acid, chlordimeform, novaluron, bistrifluron,triflumuron, diflubenzuron, imidacloprid, diazinon, acephate,endosulfan, kelevan, dimethoate, azinphos-ethyl, azinphos-methyl,izoxathion, chlorpyrifos, clofentezine, lambda-cyhalothrin, permethrin,bifenthrin, cypermethrin and the like.

Fertilizers and Micronutrients:

Fertilizers or micronutrients include, but not limited to, zinc sulfate,ferrous sulfate, ammonium sulfate, urea, urea ammonium nitrogen,ammonium thiosulfate, potassium sulfate, monoammonium phosphate, ureaphosphate, calcium nitrate, boric acid, potassium and sodium salts ofboric acid, phosphoric acid, magnesium hydroxide, manganese carbonate,calcium polysulfide, copper sulfate, manganese sulfate, iron sulfate,calcium sulfate, sodium molybdate, calcium chloride.

The pesticide or fertilizer may be a liquid or a solid. If a solid, itis preferable that it is soluble in a solvent, or the organomodifieddisiloxanes of the present invention, prior to application, and thesilicone may act as a solvent, or surfactant for such solubility oradditional surfactants may perform this function.

Agricultural Excipients:

Buffers, preservatives and other standard excipients known in the artalso may be included in the composition.

Solvents may also be included in compositions of the present invention.These solvents are in a liquid state at room temperature. Examplesinclude water, alcohols, aromatic solvents, oils (i.e. mineral oil,vegetable oil, silicone oil, and so forth), lower alkyl esters ofvegetable oils, fatty acids, ketones, glycols, polyethylene glycols,diols, paraffinics, and so forth. Particular solvents would be2,2,4-trimethyl, 1-3-pentane diol and alkoxylated (especiallyethoxylated) versions thereof as illustrated in U.S. Pat. No. 5,674,832herein incorporated by reference, or n-methyl-pyrrilidone.

Cosurfactants:

Cosurfactants useful herein include nonionic, cationic, anionic,amphoteric, zwitterionic, polymeric surfactants, or any mixture thereof.Surfactants are typically hydrocarbon based, silicone based orfluorocarbon based.

Moreover, other cosurfactants, that have short chain hydrophobes that donot interfere with superspreading as described in U.S. Pat. No.5,558,806 herein incorporated by reference are also useful.

Useful surfactants include alkoxylates, especially ethoxylates,containing block copolymers including copolymers of ethylene oxide,propylene oxide, butylene oxide, and mixtures thereof;alkylarylalkoxylates, especially ethoxylates or propoxylates and theirderivatives including alkyl phenol ethoxylate; arylarylalkoxylates,especially ethoxylates or propoxylates. and their derivatives; aminealkoxylates, especially amine ethoxylates; fatty acid alkoxylates; fattyalcohol alkoxylates; alkyl sulfonates; alkyl benzene and alkylnaphthalene sulfonates; sulfated fatty alcohols, amines or acid amides;acid esters of sodium isethionate; esters of sodium sulfosuccinate;sulfated or sulfonated fatty acid esters; petroleum sulfonates; N-acylsarcosinates; alkyl polyglycosides; alkyl ethoxylated amines; and soforth.

Specific examples include alkyl acetylenic diols (SURFONYL-AirProducts), pyrrilodone based surfactants (e.g., SURFADONE-LP 100-ISP),2-ethyl hexyl sulfate, isodecyl alcohol ethoxylates (e.g., RHODASURF DA530-Rhodia), ethylene diamine alkoxylates (TETRONICS-BASF), ethyleneoxide/propylene oxide copolymers (PLURONICS-BASF), Gemini typesurfactants (Rhodia) and diphenyl ether Gemini type surfactants (e.g.DOWFAX-Dow Chemical).

Preferred surfactants include ethylene oxide/propylene oxide copolymers(EO/PO); amine ethoxylates; alkyl polyglycosides; oxo-tridecyl alcoholethoxylates, and so forth.

In a preferred embodiment, the agrochemical composition of the presentinvention further comprises one or more agrochemical ingredients.Suitable agrochemical ingredients include, but not limited to,herbicides, insecticides, growth regulators, fungicides, miticides,acaricides, fertilizers, biologicals, plant nutritionals,micronutrients, biocides, paraffinic mineral oil, methylated seed oils(i.e. methylsoyate or methylcanolate), vegetable oils (such as soybeanoil and canola oil), water conditioning agents such as Choice® (LovelandIndustries, Greeley, Colo.) and Quest (Helena Chemical, Collierville,Tenn.), modified clays such as Surround® (Englehard Corp.,), foamcontrol agents, surfactants, wetting agents, dispersants, emulsifiers,deposition aids, antidrift components, and water.

Suitable agrochemical compositions are made by combining, in a mannerknown in the art, such as, by mixing one or more of the above componentswith the organomodified disiloxane of the present invention, either as atank-mix, or as an “In-can” formulation. The term “tank-mix” means theaddition of at least one agrochemical to a spray medium, such as wateror oil, at the point of use. The term “In-can” refers to a formulationor concentrate containing at least one agrochemical component. The“In-can” formulation may then diluted to use concentration at the pointof use, typically in a Tank-mix, or it may be used undiluted.

B. Coatings:

Typically coatings formulations will require a wetting agent orsurfactant for the purpose of emulsification, compatibilization ofcomponents, leveling, flow and reduction of surface defects.Additionally, these additives may provide improvements in the cured ordry film, such as improved abrasion resistance, antiblocking,hydrophilic, and hydrophobic properties. Coatings formulations mayexists as, Solvent-borne coatings, water-borne coatings and powdercoatings.

The coatings components may be employed as: architecture coatings; OEMproduct coatings such as automotive coatings and coil coatings; SpecialPurpose coatings such as industrial maintenance coatings and marinecoatings;

Typical resin types include: Polyesters, alkyds, acrylics, epoxies andpolyurethanes.

C. Personal Care

In a preferred embodiment, the organomodified disiloxane surfactant ofthe present invention comprises, per 100 parts by weight (“pbw”) of thepersonal care composition, from 0.1 to 99 pbw, more preferably from 0.5pbw to 30 pbw and still more preferably from 1 to 15 pbw of theorganomodified disiloxane surfactant and from 1 pbw to 99.9 pbw, morepreferably from 70 pbw to 99.5 pbw, and still more preferably from 85pbw to 99 pbw of the personal care composition.

The organomodified disiloxane surfactant compositions of the presentinvention may be utilized in personal care emulsions, such as lotions,and creams. As is generally known, emulsions comprise at least twoimmiscible phases one of which is continuous and the other which isdiscontinuous. Further emulsions may be liquids with varying viscositiesor solids. Additionally the particle size of the emulsions may renderthem microemulsions and, when sufficiently small, microemulsions may betransparent. Further it is also possible to prepare emulsions ofemulsions and these are generally known as multiple emulsions. Theseemulsions may be:

1) aqueous emulsions where the discontinuous phase comprises water andthe continuous phase comprises the organomodified disiloxane surfactantof the present invention;

2) aqueous emulsions where the discontinuous phase comprises theorganomodified disiloxane surfactant of the present invention and thecontinuous phase comprises water;

3) non-aqueous emulsions where the discontinuous phase comprises anon-aqueous hydroxylic solvent and the continuous phase comprises theorganomodified disiloxane surfactant of the present invention; and

4) non-aqueous emulsions where the continuous phase comprises anon-aqueous hydroxylic organic solvent and the discontinuous phasecomprises the organomodified disiloxane surfactant of the presentinvention.

Non-aqueous emulsions comprising a silicone phase are described in U.S.Pat. No. 6,060,546 and U.S. Pat. No. 6,271,295 the disclosures of whichare herewith and hereby specifically incorporated by reference.

As used herein the term “non-aqueous hydroxylic organic compound” meanshydroxyl containing organic compounds exemplified by alcohols, glycols,polyhydric alcohols and polymeric glycols and mixtures thereof that areliquid at room temperature, e.g. about 25° C., and about one atmospherepressure. The non-aqueous organic hydroxylic solvents are selected fromthe group consisting of hydroxyl containing organic compounds comprisingalcohols, glycols, polyhydric alcohols and polymeric glycols andmixtures thereof that are liquid at room temperature, e.g. about 25° C.,and about one atmosphere pressure. Preferably the non-aqueous hydroxylicorganic solvent is selected from the group consisting of ethyleneglycol, ethanol, propyl alcohol, iso-propyl alcohol, propylene glycol,dipropylene glycol, tripropylene glycol, butylene glycol, iso-butyleneglycol, methyl propane diol, glycerin, sorbitol, polyethylene glycol,polypropylene glycol mono alkyl ethers, polyoxyalkylene copolymers andmixtures thereof.

Once the desired form is attained whether as a silicone only phase, ananhydrous mixture comprising the silicone phase, a hydrous mixturecomprising the silicone phase, a water-in-oil emulsion, an oil-in-wateremulsion, or either of the two non-aqueous emulsions or variationsthereon, the resulting material is usually a cream or lotion withimproved deposition properties and good feel characteristics. It iscapable of being blended into formulations for hair care, skin care,antiperspirants, sunscreens, cosmetics, color cosmetics, insectrepellants, vitamin and hormone carriers, fragrance carriers and thelike.

The personal care applications where the organomodified disiloxanesurfactant of the present invention and the silicone compositionsderived therefrom of the present invention may be employed include, butare not limited to, deodorants, antiperspirants,antiperspirant/deodorants, shaving products, skin lotions, moisturizers,toners, bath products, cleansing products, hair care products such asshampoos, conditioners, mousses, styling gels, hair sprays, hair dyes,hair color products, hair bleaches, waving products, hair straighteners,manicure products such as nail polish, nail polish remover, nails creamsand lotions, cuticle softeners, protective creams such as sunscreen,insect repellent and anti-aging products, color cosmetics such aslipsticks, foundations, face powders, eye liners, eye shadows, blushes,makeup, mascaras and other personal care formulations where siliconecomponents have been conventionally added, as well as drug deliverysystems for topical application of medicinal compositions that are to beapplied to the skin.

In a preferred embodiment, the personal care composition of the presentinvention further comprises one or more personal care ingredients.Suitable personal care ingredients include, for example, emollients,moisturizers, humectants, pigments, including pearlescent pigments suchas, for example, bismuth oxychloride and titanium dioxide coated mica,colorants, fragrances, biocides, preservatives, antioxidants,anti-microbial agents, anti-fungal agents, antiperspirant agents,exfoliants, hormones, enzymes, medicinal compounds, vitamins, salts,electrolytes, alcohols, polyols, absorbing agents for ultravioletradiation, botanical extracts, surfactants, silicone oils, volatilesilicones, organic oils, waxes, film formers, thickening agents such as,for example, fumed silica or hydrated silica, particulate fillers, suchas for example, talc, kaolin, starch, modified starch, mica, nylon,clays, such as, for example, bentonite and organo-modified clays.

Suitable personal care compositions are made by combining, in a mannerknown in the art, such as, for example, by mixing, one or more of theabove components with the organomodified disiloxane surfactant. Suitablepersonal care compositions may be in the form of a single phase or inthe form of an emulsion, including oil-in-water, water-in-oil andanhydrous emulsions where the silicone phase may be either thediscontinuous phase or the continuous phase, as well as multipleemulsions, such as, for example, oil-in water-in-oil emulsions andwater-in-oil-in water-emulsions.

In one useful embodiment, an antiperspirant composition comprises theorganomodified disiloxane surfactant of the present invention and one ormore active antiperspirant agents. Suitable antiperspirant agentsinclude, for example, the Category I active antiperspirant ingredientslisted in the U.S. Food and Drug Administration's Oct. 10, 1993Monograph on antiperspirant drug products for over-the-counter humanuse, such as, for example, aluminum halides, aluminum hydroxyhalides,for example, aluminum chlorohydrate, and complexes or mixtures thereofwith zirconyl oxyhalides and zirconyl hydroxyhalides, such as forexample, aluminum-zirconium chlorohydrate, aluminum zirconium glycinecomplexes, such as, for example, aluminum zirconiumtetrachlorohydrexgly.

In another useful embodiment, a skin care composition comprises theorganomodified disiloxane surfactant, and a vehicle, such as, forexample, a silicone oil or an organic oil. The skin care compositionmay, optionally, further include emollients, such as, for example,triglyceride esters, wax esters, alkyl or alkenyl esters of fatty acidsor polyhydric alcohol esters and one or more the known componentsconventionally used in skin care compositions, such as, for example,pigments, vitamins, such as, for example, Vitamin A, Vitamin C andVitamin E, sunscreen or sunblock compounds, such as, for example,titanium dioxide, zinc oxide, oxybenzone, octylmethoxy cinnamate,butylmethoxy dibenzoylm ethane, p-aminobenzoic acid and octyldimethyl-p-aminobenzoic acid.

In another useful embodiment, a color cosmetic composition, such as, forexample, a lipstick, a makeup or a mascara composition comprises theorganomodified disiloxane surfactant, and a coloring agent, such as apigment, a water soluble dye or a liposoluble dye.

In another useful embodiment, the compositions of the present inventionare utilized in conjunction with fragrant materials. These fragrantmaterials may be fragrant compounds, encapsulated fragrant compounds, orfragrance releasing compounds that either the neat compounds or areencapsulated. Particularly compatible with the compositions of thepresent invention are the fragrance releasing silicon containingcompounds as disclosed in U.S. Pat. Nos. 6,046,156; 6,054,547;6,075,111; 6,077,923; 6,083,901; and 6,153,578; all of which are hereinand herewith specifically incorporated by reference.

The uses of the compositions of the present invention are not restrictedto personal care compositions, other products such as waxes, polishesand textiles treated with the compositions of the present invention arealso contemplated.

D. Home Care

Home care applications include laundry detergent and fabric softener,dishwashing liquids, wood and furniture polish, floor polish, tub andtile cleaners, toilet bowl cleaners, hard surface cleaners, windowcleaners, antifog agents, drain cleaners, auto-dish washing detergentsand sheeting agents, carpet cleaners, prewash spotters, rust cleanersand scale removers.

EXPERIMENTAL

The hydride intermediates for the organomodified disiloxane surfactantcompositions of the present invention, as well as comparativecompositions were prepared as described in the following examples.

Preparation Example 1

1-(2-trimethylsilylethyl)-1,1,3,3-tetramethyldisiloxane (Structure 1). A250 mL round bottom flask was charged with tetramethyldisiloxane (51.6g) and Wilkinson's catalyst ((PPh₃)₃RhCl, 100 ppm), stirred under N₂,and brought to 60° C. Trimethylvinylsilane (25.6 g) was charged to anaddition funnel, added dropwise at a rate to maintain the reactiontemperature <70° C. with cooling (˜1 g/min). The reaction was maintained1 h @ 65° C., then sampled for GC; found residual tetramethyldisiloxaneand 94:6 M′M^(R): M^(R)M^(R)). Resulting material distilled fractionallyunder vacuum (approx. 30 mm Hg) to yield 51.6 g M′M^(R) product, 99.1%GC purity. This product was found to have an Si—H content of 96 cc H₂/gby gasiometric titration.

Preparation Example 2

1-(3,3-dimethylbutyl)-1,1,3,3-tetramethyldisiloxane (Structure 2). A 250mL round bottom flask was charged with tetramethyldisiloxane (46.1 g),and stirred under N₂. A solution of Karstedt's catalyst (Pt(0) indivinyltetamethyldisiloxane, 10 ppm) in 3,3-dimethyl-1-butene (19.3 g)was charged to an addition funnel, and added dropwise at a rate tomaintain the reaction temperature <40° C. with cooling (˜0.5 g/min). Thereaction was maintained 1 h @ 50° C., then sampled for GC; foundresidual tetramethyldisiloxane, M′M^(R) product, and M^(R)M^(R)byproduct (32:53:9). Resulting material distilled fractionally undervacuum (approx. 30 mm Hg) using a 25-cm Vigreux column to yield 25.0 gM′M^(R) product, >98.1% GC purity. This product was found to have anSi—H content of 100 cc H₂/g by gasiometric titration.

Preparation Example 3

1-(2-methylpropyl)-1,1,3,3-tetramethyldisiloxane (Structure 3). An 80 mLFischer-Porter high pressure bottle was charged withtetramethyldisiloxane (10.0 g), toluene (10.0 g) and Wilkinson'scatalyst ((PPh₃)₃RhCl, 40 ppm), stirred and brought to 60° C. The bottlewas attached to a manifold and pressurized with isobutylene (25 psig)and maintained at 60-70° C. for 8 h. The pressure was vented, and thereaction was sampled for GC analysis; found residualtetramethyldisiloxane, M′MR product and MRMR byproduct (2:95:3). Theresulting material was stripped under vacuum (approx. 150 mm Hg) at 40°C. to remove olefin and M′M′, then filtered with Celite to yield 21.3 gM′M^(R) product/toluene solution, 94% GC purity. This product was foundto have an Si—H content of 11 cc H₂/g by gasiometric titration.

Preparation Example 4

1-propyl-1,1,3,3-tetramethyldisiloxane (Structure 4). An 80 mLFischer-Porter high pressure bottle was charged withtetramethyldisiloxane (10.0 g), toluene (10.0 g) and Wilkinson'scatalyst ((PPh₃)₃RhCl, 40 ppm), stirred and brought to 50° C. The bottlewas attached to a manifold and pressurized with propylene (40 psig) andmaintained at 50° C. for 2 h. The pressure was vented, and the reactionwas sampled for GC analysis; found M′M^(R) product and M^(R)M^(R)byproduct (40:60). The resulting mixture of materials was used withoutfurther purification, yield 140.1 g.

Preparation Example 5

1-tert-butyl-1,1,3,3-tetramethyldisiloxane (Structure 5). A 1 L roundbottom flask was charged with water (95 g) and diisopropyl ether (50 g)and stirred. A solution of tert-butyldimethylsilyl chloride (39.5 g) inisopropyl ether (50 g) was charged to an addition funnel, and addeddropwise to the water/IPE mixture at a rate to maintain the reactiontemperature between 30-35° C. After complete addition, the reactiontemperature was brought to 40° C. and maintained for 1 h. A solution ofdimethylchlorosilane (24.8 g) in isopropyl ether (50 g) was then chargedto the addition funnel, and this solution was added dropwise at 40-45°C. After complete addition, the reaction mixture was heated to refluxfor 1 h and allowed to cool. After aqueous workup (washing with waterand aqueous NaHCO₃, and drying organic fractions over MgSO₄), theproduct was isolated by fractional distillation under vacuum to yield39.2 g M(R)M′ product/isopropyl ether solution (70%/20% by GC analysis).This product was found to have an Si—H content of 79 cc H₂/g bygasiometric titration.

Preparation Example 6

1-(dicyclopentadienyl)-1,1,3,3-tetramethyldisiloxane (Structure 6). A250 mL RBF was charged with tetramethyldisiloxane (45.3 g), stirredunder N₂, and brought to 40° C. A solution of Karstedt's catalyst (Pt(0)in divinyltetamethyldisiloxane, 40 ppm) in dicyclolpentadiene (29.8 g)was charged to an addition funnel, and added dropwise at a rate tomaintain the reaction temperature <60° C. with cooling (˜0.5 g/min).After complete addition, the reaction was maintained 1 h @ 60° C. Thereaction mixture was stripped in vacuo (˜30 mm Hg) at 100° C. to yield41.1 g M′M^(R) product, >96% GC purity. This product was found to havean Si—H content of 81 cc H₂/g by gasiometric titration.

Preparation Example 7

The hydride intermediates of Examples 1-6 were further modified withvarious allylpolyalkyleneoxides to yield the organomodified disiloxanecompositions of this instant invention (From Examples 1, 2, 3 and 5), aswell as the comparative disiloxane surfactants (From Examples 4 and 6).

Additionally comparative trisiloxane alkoxylates were prepared byconventional methods of platinum mediated hydrosilation, as described inBailey, U.S. Pat. No. 3,299,112, herein incorporated by reference.

Table 1 provides a description of the compositions of the presentinvention. These compositions are described by the general structure:M*M″where M*═R¹Si(CH₃)₂O_(0.5); M″═O_(0.5)Si(CH₃)₂Qwhere R¹ is described in Table 2;

Q=—CH₂CH₂CH₂O(CH₂CH₂O)_(a)(CH₂CH(CH₃)O)_(b)R² TABLE 1 Description ofOrganomodified Disiloxane Surfactant Compositions I.D. R¹ a b R² 1(CH₃)₂CHCH₂— 7.5 0 CH₃ 2 CH₃CH₂CH₂— 7.5 0 CH₃ 3 (CH₃)₂CHCH₂— 7.5 0 H 4(CH₃)₂CHCH₂— 11 0 H 5 (CH₃)₃C— 7.5 0 CH₃ 6 (CH₃)₂CHCH₂— 7.5 0 H 7(CH₃)₂CHCH₂— 11 0 H 8 (CH₃)₂CHCH₂— 7.5 0 CH₃ 9 (CH₃)₃SiCH₂CH₂— 7.5 0 H10 (CH₃)₃SiCH₂CH₂— 7.5 0 CH₃ 11 (CH₃)₃SiCH₂CH₂— 11 0 H 12(CH₃)₃SiCH₂CH₂— 5 2.5 H 13 (CH₃)₃SiCH₂CH₂— 6.3 0 H

TABLE 2 Comparative Siloxane Based Surfactants I.D. R¹ a b R² A CH₃— 7.50 H B CH₃— 7.5 0 CH₃ C CH₃— 11 0 H D

11 0 H H

7.5 0 HTable 3 provides a description of the comparative organosiliconepolyether based surfactants of the general structure:

where Z=—CH₂CH₂CH₂O(CH₂CH₂O)_(a)(CH₂CH(CH₃)O)_(b)R² TABLE 3 Compositionof Comparative Organosilicone Polyether Surfactants Z Group I.D. x y a bR² E 0 1 7.5 0 CH₃ F 0 1 7.5 0 H G 20 3 7.5 0 CH₃

Additionally, comparative sample OPE (Octylphenolethoxylate, containing10 polyoxyethylene units) is a non-silicone organic surfactant. Thisproduct is available as Triton® X-100 from Dow Chemical Company,Midland, Mich.

Example 8

This example demonstrates the ability of the organomodified disiloxanecomposition of the present invention to reduce aqueous surface tensionthereby showing utility as surfactants. Surface tension was measuredusing a Kruss surface tensiometer, with a sand blasted platinum blade asthe sensor. Solutions of the various components were prepared at 0.1 wt% in 0.005M NaCl water (Deionized), as an equilibrium aid.

Table 4 shows that solutions of these unique compositions provide asignificant reduction in surface tension relative to the conventionalsurfactant.

The compositions of the present invention also provide spreadingproperties similar to the TSAs (E and F), and comparative disiloxanesurfactants (A, B, C, D and H). Additionally, organomodified disiloxanesurfactants of the present invention provide improved spreading relativeto the conventional silicone polyether (G) and conventional organicsurfactant product OPE (Table 4).

Spreading was determined by applying a 10 μL droplet, of surfactantsolution to polyacetate film (USI, “Crystal Clear Write on Film”) andmeasuring the spread diameter (mm) after 30 seconds, at a relativehumidity between 50 and 70% (at 22 to 25° C.). The solution was appliedwith an automatic pipette to provide droplets of reproducible volume.Deionized water that was further purified with a Millipore filtrationsystem was used to prepare the surfactant solutions. TABLE 4 SurfaceTension and Spreading Properties Surface Spread Diameter (mm) I.D.Tension mN/m 0.1% 0.2% 0.4% 1 23.3 40 42 50 2 23.6 34 36 33 3 24.0 12 1424 4 24.1 8 9 10 5 23.5 32 48 45 6 23.2 41 33 23 7 23.9 14 15 25 8 24.023 33 41 9 22.8 14 25 49 10 23.0 15 27 34 11 24.5 20 21 32 12 24.3 7 810 13 22.2 14 32 27 A 23.4 8 36 58 B 24.3 8 12 44 C 24.1 6 8 9 D 32.7 7nd nd E 20.9 53 51 25 F 20.6 53 50 35 G 23.6 nd nd 6 H nd nd nd 7 OPE31.8 nd nd 10

Example 9

Hydrolytic stability was determined for representative compositions ofthe present invention using HPLC. Solutions of the various compositionswere prepared at 0.5 wt % over a pH range from pH 4 to pH12, andmonitored by HPLC for decomposition as a function of time.

Analytical Method:

The samples were analyzed by a reverse-phase chromatographic techniqueusing the experimental conditions listed in Table 5. TABLE 5 SolventGradient for HPLC Method Time (min.) % Methanol % Water % Isopropanol0.0 70 30 0 15.0 100 0 0 20.0 50 0 50 20.1 70 30 0 25.0 70 30 0

-   Detector: ELSD/LTA (Evaporative Light Scattering with Low    Temperature Adapter-   Conditions: 30° C., 1.95 SLPM N₂-   Column: Phenomenex LUNA C18 end cap, 5 micron, 75×4.6 mm-   Flow Rate: 1.0 mL/min.-   Inj. Volume: 10 microlitres-   Sample: 0.050 g/mL in methanol

Tables 6-16 demonstrates that the compositions of the present inventionprovide improved resistance to hydrolytic decomposition relative to thestandard comparative siloxane-based surfactants siloxanes B and E undersimilar pH conditions.

Comparative siloxanes B and E show rapid hydrolysis at ≦pH5 and >pH 7,while the organomodified disiloxane surfactants of the present inventiondemonstrate a higher resistance to hydrolysis under the same conditions.

Although comparative D shows similar resistance to hydrolysis, it doesnot provide the enhanced spreading properties associated with theorganomodified disiloxane surfactants of the present invention. Forexample comparative D gave a spread diameter of only 6 mm (0.4%) and had82% product remaining by HPLC, after 48 h at pH4, while theorganomodified disiloxane surfactant product 10 gave a spread diameterof 34 mm and maintained 75% product after 1 week, under the sameconditions (Tables 4, 11 and 16). TABLE 6 Hydrolytic Stability ofSiloxane Based Surfactants by HPLC Stability: % Siloxane SurfactantRemaining I.D. Time pH 4 pH 5 pH 7 pH 9 pH 10 pH 11 pH 12 1 24 h 83 100100 100 100 100 nd 1 wk 8 71 100 100 100 68 nd 2.5 wk 1 38 100 100 83 35nd 15 wk 0.5 4 100 100 42 28 nd

TABLE 7 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 2 24 h 23 88 100 100 100 79 nd 1 wk 1 26 100 95 69 17nd 2.5 wk 0 7 100 89 44 7 nd

TABLE 8 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 5 1 wk 65 100 100 100 100 100 nd 4 wk 32 76 100 100100 100 nd 6 wk 21 64 100 100 100 100 nd

TABLE 9 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 8 24 h 84 100 100 100 100 nd nd 1 wk 50 100 100 100100 nd nd 2 wk 31 79 100 100 100 nd nd 4 wk 21 65 100 97 88 nd nd 10 wk7 45 100 93 83 nd nd

TABLE 10 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 9 24 h 92 100 100 100 100 nd nd 1 wk 67 100 100 100100 nd nd

TABLE 11 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 10 24 h 100 100 100 100 100 100 79 1 wk 75 100 100 100100 93 42 2 wk 50 88 100 100 100 nd nd 3 wk 32 80 100 100 100 93 34 7 wknd nd nd nd nd 93 11 7.5 wk 12 56 100 100 100 nd nd 11 wk nd 48 100 100100 nd nd 13 wk nd nd nd nd nd 95 nd 17 wk nd nd 100 100 84 nd nd 27 wknd nd 100 100 86 100 nd

TABLE 12 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 11 96 h 100 100 100 100 100 nd nd 3 wk 79 100 100 100100 nd nd 6 wk 56 100 100 100 100 nd nd 11 wk 10 100 100 100 100 nd ndNote:Stock Solution 2.5 wt %

TABLE 13 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 13 24 h 100 100 100 100 100 nd nd 1 wk 56 100 100 100100 nd nd

TABLE 14 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 E 48 h 25 100 100 100 46 nd nd 1 wk 0 38 100 53 0 ndnd

TABLE 15 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 B 24 h 0 0 100 38 0 nd nd

TABLE 16 Hydrolytic Stability of Siloxane Based Surfactants by HPLCStability: % Siloxane Surfactant Remaining I.D. Time pH 4 pH 5 pH 7 pH 9pH 10 pH 11 pH 12 D 48 h 82 >95 >95 >95 >95 nd nd 9 days 44 99 99 99 99nd nd

Examples 10-12

Unlike traditional siloxane based surfactants, which are subject torapid hydrolysis under acidic and basic conditions (≦pH 5 and ≧pH 9) theorganomodified disiloxane surfactants of the present invention provideincreased resistance to hydrolysis relative to traditional trisiloxanealkoxylates (Comparative E and F), as well as the comparativetrimethylsilyl terminated disiloxane surfactants, represented byComparative B. An artifact of hydrolysis is observed as a reduction insuperpsreading properties over time. Therefore solutions of theorganomodified disiloxane surfactants of the present invention, as wellas comparative surfactants were prepared at desired use levels and pH.Spreading was determined as a function of time to illustrate resistanceto hydrolysis.

Example 10

Table 17 is an illustrative example of the organomodified disiloxanesurfactants, where product No. 10, has improved resistance tohydrolysis, at pH 3, relative to a traditional trisiloxane ethoxylatesuperspreading surfactant (Product E). As mentioned above, resistance tohydrolysis was observed by monitoring the spreading properties overtime. Here a 0.4 wt % solution was prepared at pH 3, and spreadingdetermined according to the procedure in Example 8. TABLE 17 SpreadingProperties at pH 3 vs Time (h) Time/Spread Diameter (mm) I.D 0 h 0.25 h0.5 h 1 h 2 h 4 h 8 h 24 h 32 h 96 h 10 32 39 41 49 48 39 39 36 16 19 E48 48 43 42 44 12 12 9 — —

Example 11

In another example the organomodified disiloxane surfactants of thepresent invention represented by product Nos. 6 and 11, demonstrateimproved resistance to hydrolysis relative to product F, a trisiloxaneethoxylate superspreader (Table 18). Solutions (0.4 wt %) of thesurfactants were prepared at pH 4 and pH 5 and spreading properties wereobserved over time. The test conditions are outlined in Example 8. TABLE18 Spreading Properties at pH 4 and pH 5 Vs Time Spreading Diameter (mm)ID: 6 6 11 11 F F Time pH 4 pH 5 pH 4 pH 5 pH 4 pH 5 0 h 50 46 16 26 5049 1 h 48 44 23 23 50 50 4 h 59 48 23 — 46 47 24 h 49 51 44 24 52 51 48h 40 49 38 32 39 49 72 h 42 50 28 35 16 48 1 wk 13 43 8 29 12 52 2 wk 1149 8 33 7 53 3 wk 18 47 12 33 6 21 1 mo 17 49 10 42 6 15

Example 12

In another example the organomodified disiloxane surfactants of thepresent invention, represented by product No. 5, shows improvedresistance to hydrolysis relative to comparative product E. Heresurfactant solutions (0.1 wt %) were prepared at pH 4, pH 5, pH 8, pH 9and pH 10, and the spreading properties over time were observed asdescribed in Example 8.

Table 19 demonstrates that the comparative silicone E shows a more rapidloss of spreading properties at pH 4, pH 5, pH 9 and pH 10, than productNo. 5. TABLE 19 Spreading Properties vs. Time Spread Diameter (mm) TimeProduct pH 4 pH 5 pH 8 pH 9 pH 10 0 h 5 53 52 52 51 51 E 56 54 56 54 541 h 5 52 50 51 50 51 E 55 53 53 56 54 2 h 5 54 52 50 49 50 E 51 53 55 5552 4 h 5 51 50 50 48 49 E 41 51 56 53 49 6 h 5 51 50 50 48 49 E 35 52 5053 46 8 h 5 48 51 52 49 52 E 29 50 51 51 47 24 h 5 51 50 52 51 49 E 7 5053 50 32 48 h 5 39 48 46 46 41 E 6 41 47 43 10 72 h 5 33 48 45 45 42 E 632 49 44 7 96 h 5 23 45 47 46 40 E 6 17 50 41 6 168 h 5 8 43 43 44 43 E5 9 50 32 6

Example 13

The impact of other ingredients on spreading was determined by blendingthe organosilicone disiloxane surfactant of the present invention, witha conventional organic based cosurfactant. The cosurfactants aredescribed in Table 20.

Blends were prepared as physical mixtures where the weight fractionsilicone is represented by α (alpha), indicating that the cosurfactantmakes up the balance of the blend ratio. For example when α=0 thisindicates that the composition contains 0% of the silicone component and100% cosurfactant, while an α=1.0 indicates the composition contains100% silicone, and no (0%) cosurfactant. Mixtures of the two componentsare represented by the weight fraction α, where α ranges as follows:0≦α≦1.0. By example when α=0.25 this indicates the surfactant mixture iscomposed of 25% silicone and 75% cosurfactant. These blends are thendiluted in water to the desired concentration for spreading evaluation.

Spreading was determined as described in Example 8, at either 0.1 wt %or 0.2 wt % total surfactant.

Table 21 demonstrates that representative examples of the cosurfactantsof the present invention provide favorable spreading results, and insome cases provide an unexpected synergistic enhancement, where thespread diameter of the mixture exceeds that of the individualcomponents. TABLE 20 Description of Conventional Cosurfactants IDDescription IDA-5 Isodecyl alcohol ethoxylate (4-5 EO) IDA-6 Isodecylalcohol ethoxylate (5-6 EO) TMN-6 Trimethylnonylalcohol ethoxylate (6EO) Oxo-TDA-5 Oxo-tridecyl alcohol ethoxylate (5 EO) Oxo-TDA-6Oxo-tridecyl alcohol ethoxylate (6 EO) APG C₈₋₁₀ Alkylpolyglucoside

TABLE 21 Effect of Cosurfactants on Blend Spreading Properties WtFraction (α) Silicone Surfactant Spread diameter (mm) Run Silicone 00.25 0.50 0.75 1.0 Cosurfactant 1 10 ^(a) 45 49 23 17 25 IDA-5 2 10 ^(a)35 38 47 26 25 IDA-6 3 10 ^(a) 41 38 42 36 25 TMN-6 4 10 ^(a) 34 29 2319 25 Oxo-TDA-5 5 10 ^(a) 39 42 49 36 25 Oxo-TDA-6 6 10 ^(a) 10 39 42 3525 APG 7  5 ^(b) 41 46 47 49 50 IDA-5 8  5 ^(b) 19 31 35 46 50 IDA-6 9 5 ^(b) 34 38 44 45 50 TMN-6 10  5 ^(b) 36 40 44 51 50 Oxo-TDA-5 11  5^(b) 38 40 39 46 50 Oxo-TDA-6 12  5 ^(b) 8 32 40 48 50 APG^(a) = 0.2 wt % total surfactant^(b) = 0.1 wt % total surfactant

The foregoing examples are merely illustrative of the invention, servingto illustrate only some of the features of the present invention. Theappended claims are intended to claim the invention as broadly as it hasbeen conceived and the examples herein presented are illustrative ofselected embodiments from a manifold of all possible embodiments.Accordingly it is Applicants' intention that the appended claims are notto be limited by the choice of examples utilized to illustrate featuresof the present invention. As used in the claims, the word “comprises”and its grammatical variants logically also subtend and include phrasesof varying and differing extent such as for example, but not limitedthereto, “consisting essentially of” and “consisting of.” Wherenecessary, ranges have been supplied; those ranges are inclusive of allsub-ranges there between. Such ranges may be viewed as a Markush groupor groups consisting of differing pairwise numerical limitations whichgroup or groups is or are fully defined by its lower and upper bounds,increasing in a regular fashion numerically from lower bounds to upperbounds. It is to be expected that variations in these ranges willsuggest themselves to a practitioner having ordinary skill in the artand where not already dedicated to the public, those variations shouldwhere possible be construed to be covered by the appended claims. It isalso anticipated that advances in science and technology will makeequivalents and substitutions possible that are not now contemplated byreason of the imprecision of language and these variations should alsobe construed where possible to be covered by the appended claims. AllUnited States patents (and patent applications) referenced herein areherewith and hereby specifically incorporated by reference in theirentirety as though set forth in full.

1. An agricultural composition comprising: a) a silicone having theformula:MM′ where M=R¹R²R³SiO_(1/2); M=R⁴R⁵R⁶SiO_(1/2); with R¹ selected fromthe group consisting of branched monovalent hydrocarbon radical of from3 to 6 carbon atoms and R⁷, where R⁷ is selected from the groupconsisting of R⁸R⁹R¹⁰SiR¹² and (R⁴R⁵R⁶)SiR¹² with R⁸, R⁹, and R¹⁰ eachindependently selected from the group of monovalent hydrocarbon radicalshaving from 1 to 6 carbon atoms and monovalent aryl or alkarylhydrocarbon radicals having from 6 to 13 carbon atoms and R¹² is adivalent hydrocarbon radical having from 1 to 3 carbon atoms, R² and R³are each independently selected from the group of from 1 to 6 carbonatom monovalent hydrocarbon radicals or R¹, with R⁴ analkylpolyalkyleneoxide bearing substituent selected from the groupconsisting of: R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴ andR¹²SiR⁵R⁶(R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R₁₄) where R¹³ is adivalent linear or branched hydrocarbon radical having the structure:—CH₂—CH(R¹⁵)(R¹⁶)_(d)O— where R¹⁵ is H or methyl; R¹⁶ is a divalentalkyl radical of 1 to 6 carbons where the subscript d may be 0 or 1; R¹⁴is selected from the group consisting of H, monovalent hydrocarbonradicals of from 1 to 6 carbon atoms and acetyl where the subscripts a,b and c are zero or positive and satisfy the following relationships:2≦a+b+c≦20 with a≧2, and R⁵ and R⁶ are each independently selected fromthe group of monovalent hydrocarbon radicals having from 1 to 6 carbonatoms or R⁴; and b) an agriculturally active component selected from thegroup consisting of pesticides, fungicides, insecticides, herbicides andfertilizers wherein said agricultural composition has an enhancedresistance to hydrolysis.
 2. The composition of claim 1 where R¹ isiso-propyl.
 3. The composition of claim 1 where R¹ is iso-butyl.
 4. Thecomposition of claim 1 where R¹ is tert-butyl.
 5. The composition ofclaim 1 where R¹ is R⁷ where R⁷ has the formula: R⁸R⁹R¹⁰SiR¹² with R⁸,R⁹, and R¹⁰ each methyl and R¹² is a divalent hydrocarbon radical having2 carbon atoms.
 6. The composition of claim 1 where R¹⁵ is hydrogen. 7.The composition of claim 1 where R² is methyl.
 8. The composition ofclaim 2 where R¹⁵ is hydrogen.
 9. The composition of claim 2 where R² ismethyl.
 10. The composition of claim 3 where R¹⁵ is hydrogen.
 11. Thecomposition of claim 3 where R² is methyl.
 12. The composition of claim4 where R¹⁵ is hydrogen.
 13. The composition of claim 4 where R² ismethyl.
 14. The composition of claim 5 where R¹⁵ is hydrogen.
 15. Thecomposition of claim 5 where R² is methyl.
 16. An aqueous emulsionwherein the discontinuous phase comprises water and the continuous phasecomprises the composition of claim
 1. 17. An aqueous emulsion whereinthe continuous phase comprises water and the discontinuous phasecomprises the composition of claim
 1. 18. A non-aqueous emulsion whereinthe discontinuous phase comprises a non-aqueous hydroxylic solvent andthe continuous phase comprises the composition of claim
 1. 19. Anon-aqueous emulsion wherein the continuous phase comprises anon-aqueous hydroxylic solvent and the discontinuous phase comprises thecomposition of claim
 1. 20. The composition of claim 1 wherein thepesticide is selected from the group consisting of rodenticides,insecticides, miticides, fungicides, and herbicides.
 21. The compositionof claim 1 wherein the fungicide is selected from the group consistingof aldimorph, tridemorph, dodemorph, dimethomorph; flusilazol,azaconazole, cyproconazole, epoxiconazole, furconazole, propiconazole,tebuconazole, imazalil, thiophanate, benomyl carbendazim,chlorothialonil, dicloran, trifloxystrobin, fluoxystrobin,dimoxystrobin, azoxystrobin, furcaranil, prochloraz, flusulfamide,famoxadone, captan, maneb, mancozeb, dodicin, dodine, and metalaxyl. 22.The composition of claim 1 wherein the insecticide is selected from thegroup consisting of bacillus thuringiensis, spinosad, abamectin,doramectin, lepimectin, pyrethrins, carbaryl, primicarb, aldicarb,methomyl, amitraz, boric acid, chlordimeform, novaluron, bistrifluron,triflumuron, diflubenzuron, imidacloprid, diazinon, acephate,endosulfan, kelevan, dimethoate, azinphos-ethyl, azinphos-methyl,izoxathion, chlorpyrifos, clofentezine, lambda-cyhalothrin, permethrin,bifenthrin, and cypermethrin.
 23. The composition of claim 1 wherein theherbicide is selected from the group consisting of phenoxy acetic acids,phenoxy propionic acids, phenoxy butyric acids, benzoic acids, triazinesand s-triazines, substituted ureas, uracils, bentazon, desmedipham,methazole, phenmedipham, pyridate, amitrole, clomazone, fluridone,norflurazone, dinitroanilines, isopropalin, oryzalin, pendimethalin,prodiamine, trifluralin, glyphosate, sulfonylureas, imidazolinones,clethodim, diclofop-methyl, fenoxaprop-ethyl, fluazifop-p-butyl,haloxyfop-methyl, quizalofop, sethoxydim, dichlobenil, isoxaben, andbipyridylium compounds.
 24. The composition of claim 1 wherein thefertilizer is selected from the group consisting of zinc sulfate,ferrous sulfate, ammonium sulfate, urea, urea ammonium nitrogen,ammonium thiosulfate, potassium sulfate, monoammonium phosphate, ureaphosphate, calcium nitrate, boric acid, potassium salts of boric acid,sodium salts of boric acid, phosphoric acid, magnesium hydroxide,manganese carbonate, calcium polysulfide, copper sulfate, manganesesulfate, iron sulfate, calcium sulfate, sodium molybdate, and calciumchloride.
 25. A cosmetic composition comprising: a) a silicone havingthe formula:MM′ where M=R¹R²R³SiO_(1/2); M′═R⁴R⁵R⁶SiO_(1/2); with R¹ selected fromthe group consisting of branched monovalent hydrocarbon radical of from3 to 6 carbon atoms and R⁷, where R⁷ is selected from the groupconsisting of R⁸R⁹R¹⁰SiR¹² and (R⁴R⁵R⁶)SiR¹² with R⁸, R⁹, and R¹⁰ eachindependently selected from the group of monovalent hydrocarbon radicalshaving from 1 to 6 carbon atoms and monovalent aryl or alkarylhydrocarbon radicals having from 6 to 13 carbon atoms and R¹² is adivalent hydrocarbon radical having from 1 to 3 carbon atoms, R² and R³are each independently selected from the group of from 1 to 6 carbonatom monovalent hydrocarbon radicals or R¹, with R⁴ analkylpolyalkyleneoxide bearing substituent selected from the groupconsisting of: R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴ andR¹²SiR⁵R⁶(R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴) where R¹³ is adivalent linear or branched hydrocarbon radical having the structure:—CH₂—CH(R¹⁵)(R¹⁶)_(d)O— where R¹⁵ is H or methyl; R¹⁶ is a divalentalkyl radical of 1 to 6 carbons where the subscript d may be 0 or 1; R¹⁴is selected from the group consisting of H, monovalent hydrocarbonradicals of from 1 to 6 carbon atoms and acetyl where the subscripts a,b and c are zero or positive and satisfy the following relationships:2≦a+b+c≦20 with a≧2, and R⁵ and R⁶ are each independently selected fromthe group of monovalent hydrocarbon radicals having from 1 to 6 carbonatoms or R⁴; and b) a personal care ingredient wherein said cosmeticcomposition has an enhanced resistance to hydrolysis.
 26. Thecomposition of claim 25 where R¹ is iso-propyl.
 27. The composition ofclaim 25 where R¹ is iso-butyl.
 28. The composition of claim 25 where R¹is tert-butyl.
 29. The composition of claim 25 where R¹ is R⁷ where R⁷has the formula: R⁸R⁹R¹⁰SiR¹² with R⁸, R⁹, and R¹⁰ each methyl and R¹²is a divalent hydrocarbon radical having 2 carbon atoms.
 30. Thecomposition of claim 25 where R¹⁵ is hydrogen.
 31. The composition ofclaim 25 where R² is methyl.
 32. The composition of claim 26 where R¹⁵is hydrogen.
 33. The composition of claim 26 where R² is methyl.
 34. Thecomposition of claim 27 where R¹⁵ is hydrogen.
 35. The composition ofclaim 27 where R² is methyl.
 36. The composition of claim 28 where R¹⁵is hydrogen.
 37. The composition of claim 28 where R² is methyl.
 38. Thecomposition of claim 29 where R¹⁵ is hydrogen.
 39. The composition ofclaim 29 where R² is methyl.
 40. An aqueous emulsion wherein thediscontinuous phase comprises water and the continuous phase comprisesthe composition of claim
 25. 41. An aqueous emulsion wherein thecontinuous phase comprises water and the discontinuous phase comprisesthe composition of claim
 25. 42. A non-aqueous emulsion wherein thediscontinuous phase comprises a non-aqueous hydroxylic solvent and thecontinuous phase comprises the composition of claim
 25. 43. Anon-aqueous emulsion wherein the continuous phase comprises anon-aqueous hydroxylic solvent and the discontinuous phase comprises thecomposition of claim
 25. 44. The composition of claim 25 wherein thepersonal care ingredient is selected from the group consisting ofemollients, moisturizers, humectants, pigments, pearlescent pigments,bismuth oxychloride, titanium dioxide coated mica, colorants,fragrances, biocides, preservatives, antioxidants, anti-microbialagents, anti-fungal agents, antiperspirant agents, exfoliants, hormones,enzymes, medicinal compounds, vitamins, salts, electrolytes, alcohols,polyols, ultraviolet radiation absorbing agents, botanical extracts,surfactants, silicone oils, volatile silicones, organic oils, waxes,film formers, thickening agents, fumed silica, hydrated silica,particulate fillers, talc, kaolin, starch, modified starch, mica, nylon,clays, bentonite and organo-modified clays.
 45. A coating compositioncomprising: a) a silicone having the formula:MM′ where M=R¹R²R³SiO_(1/2); M=R⁴R⁵R⁶SiO_(1/2); with R¹ selected fromthe group consisting of branched monovalent hydrocarbon radical of from3 to 6 carbon atoms and R⁷, where R⁷ is selected from the groupconsisting of R⁸R⁹R¹⁰SiR¹² and (R⁴R⁵R⁶)SiR¹² with R⁸, R⁹, and R¹⁰ eachindependently selected from the group of monovalent hydrocarbon radicalshaving from 1 to 6 carbon atoms and monovalent aryl or alkarylhydrocarbon radicals having from 6 to 13 carbon atoms and R¹² is adivalent hydrocarbon radical having from 1 to 3 carbon atoms, R² and R³are each independently selected from the group of from 1 to 6 carbonatom monovalent hydrocarbon radicals or R¹, with R⁴ analkylpolyalkyleneoxide bearing substituent selected from the groupconsisting of: R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴ andR¹²SiR⁵R⁶(R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴) where R¹³ is adivalent linear or branched hydrocarbon radical having the structure:—CH₂—CH(R¹⁵)(R¹⁶)_(d)O— where R¹⁵ is H or methyl; R¹⁶ is a divalentalkyl radical of 1 to 6 carbons where the subscript d may be 0 or 1; R¹⁴is selected from the group consisting of H, monovalent hydrocarbonradicals of from 1 to 6 carbon atoms and acetyl where the subscripts a,b and c are zero or positive and satisfy the following relationships:2≦a+b+c≦20 with a≧2, and R⁵ and R⁶ are each independently selected fromthe group of monovalent hydrocarbon radicals having from 1 to 6 carbonatoms or R⁴; and b) a coating resin selected from the group consistingof polyesters, alkyds, acrylics, epoxies, and polyurethanes wherein saidcoating composition has an enhanced resistance to hydrolysis.
 46. A homecare composition comprising: a) a silicone having the formula:MM′ where M=R¹R²R³SiO_(1/2); M′═R⁴R⁵R⁶SiO_(1/2); with R¹ selected fromthe group consisting of branched monovalent hydrocarbon radical of from3 to 6 carbon atoms and R⁷, where R⁷ is selected from the groupconsisting of R⁸R⁹R¹⁰SiR¹² and (R⁴R⁵R⁶)SiR¹² with R⁸, R⁹, and R¹⁰ eachindependently selected from the group of monovalent hydrocarbon radicalshaving from 1 to 6 carbon atoms and monovalent aryl or alkarylhydrocarbon radicals having from 6 to 13 carbon atoms and R¹² is adivalent hydrocarbon radical having from 1 to 3 carbon atoms, R² and R³are each independently selected from the group of from 1 to 6 carbonatom monovalent hydrocarbon radicals or R¹, with R⁴ analkylpolyalkyleneoxide bearing substituent selected from the groupconsisting of: R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴ andR¹²SiR⁵R⁶(R¹³(C₂H₄O)_(a)(C₃H₆O)_(b)(C₄H₈O)_(c)R¹⁴) where R¹³ is adivalent linear or branched hydrocarbon radical having the structure:—CH₂—CH(R¹⁵)(R¹⁶)_(d)O— where R¹⁵ is H or methyl; R¹⁶ is a divalentalkyl radical of 1 to 6 carbons where the subscript d may be 0 or 1; R¹⁴is selected from the group consisting of H, monovalent hydrocarbonradicals of from 1 to 6 carbon atoms and acetyl where the subscripts a,b and c are zero or positive and satisfy the following relationships:2≦a+b+c≦20 with a≧2, and R⁵ and R⁶ are each independently selected fromthe group of monovalent hydrocarbon radicals having from 1 to 6 carbonatoms or R⁴; and b) a surfactant wherein said home care composition hasan enhanced resistance to hydrolysis.
 47. The composition of claim 46where R¹ is iso-propyl.
 48. The composition of claim 46 where R¹ isiso-butyl.
 49. The composition of claim 46 where R¹ is tert-butyl. 50.The composition of claim 46 where R¹ is R⁷ where R⁷ has the formula:R⁸R⁹R¹⁰SiR¹² with R⁸, R⁹, and R¹⁰ each methyl and R¹² is a divalenthydrocarbon radical having 2 carbon atoms.
 51. The composition of claim46 where R¹⁵ is hydrogen.
 52. The composition of claim 46 where R² ismethyl.
 53. The composition of claim 47 where R¹⁵ is hydrogen.
 54. Thecomposition of claim 47 where R² is methyl.
 55. The composition of claim48 where R¹⁵ is hydrogen.
 56. The composition of claim 48 where R² ismethyl.
 57. The composition of claim 49 where R¹⁵ is hydrogen.
 58. Thecomposition of claim 49 where R² is methyl.
 59. The composition of claim50 where R¹⁵ is hydrogen.
 60. The composition of claim 50 where R² ismethyl.
 61. An aqueous emulsion wherein the discontinuous phasecomprises water and the continuous phase comprises the composition ofclaim
 46. 62. An aqueous emulsion wherein the continuous phase compriseswater and the discontinuous phase comprises the composition of claim 46.63. A non-aqueous emulsion wherein the discontinuous phase comprises anon-aqueous hydroxylic solvent and the continuous phase comprises thecomposition of claim
 46. 64. A non-aqueous emulsion wherein thecontinuous phase comprises a non-aqueous hydroxylic solvent and thediscontinuous phase comprises the composition of claim
 46. 65. Thecomposition of claim 46 wherein the surfactant is selected from thegroup consisting of alkoxylates, ethoxylates, block copolymers ofethylene oxide, copolymers of ethylene oxide, copolymers of propyleneoxide, copolymers of butylene oxide, alkyl phenol ethoxylate, alkylphenol propoxylate, arylarylalkoxylates, amine alkoxylates, amineethoxylates; fatty acid alkoxylates; fatty alcohol alkoxylates; alkylsulfonates; alkyl benzene sulfonates, alkyl naphthalene sulfonates;sulfated fatty alcohols, sulfated fatty alcohols, sulfated fatty amines,sulfated fatty acid amides; acid esters of sodium isethionate; esters ofsodium sulfosuccinate; sulfated fatty acid esters, sulfonated fatty acidesters, petroleum sulfonates, N-acyl sarcosinates; alkyl polyglycosides;alkyl ethoxylated amines, alkyl acetylenic diols, pyrrilodone basedsurfactants, 2-ethyl hexyl sulfate, isodecyl alcohol ethoxylates,ethylene diamine alkoxylates, ethylene oxide/propylene oxide copolymers,diphenyl ether Gemini type surfactants, ethylene oxide/propylene oxidecopolymers (EO/PO); amine ethoxylates; alkyl polyglycosides;oxo-tridecyl alcohol ethoxylates, and mixtures thereof.